Cookie policy: This site uses cookies (small files stored on your computer) to simplify and improve your experience of this website. Cookies are small text files stored on the device you are using to access this website. For more information please take a look at our terms and conditions. Some parts of the site may not work properly if you choose not to accept cookies.


Subscribe or Register

Existing user? Login


An update on epidural anaesthesia

By Lee Wilson, MSc, MRPharmS, and Donald Graham, MBChB, FRCA


This series offers a simple, practical approach to continuing education.

Plan your learning using the “Objectives”, use the “Discussion points” to reflect on what you have read and “Test yourself” with the multiple-choice questions found below.

Why not try it with a group of colleagues at lunchtime?

Answers at the bottom of page 2 PDF

Regional anaesthesia differs from general anaesthesia in that it is used to target a specific part of the body. The term encompasses the use of local anaesthetic drugs (often in combination with low-dose opioids) in central neuraxial blocks and peripheral nerve blocks. This article focuses on the use of central neuraxial blocks, specifically epidurals.

Central neuraxial blockade

Spinal and epidural anaesthesia are collectively termed “central neuraxial blockade” (CNB). Spinal (or intrathecal) anaesthesia involves injecting a local anaesthetic, with or without an opioid, into the cerebrospinal fluid in the subarachnoid space. If the drugs are injectedor infused into the epidural space surrounding the spinal fluid sac this is termed epidural anaesthesia. The extent and height of the block are determined by the volume and concentration of drug that is used and the site of catheter insertion.

CNB is often used in obstetrics, and is used in some 8–10% of all operations in the UK1 (examples include major thoracic, abdominal or lower-limb surgery).

The “Third national audit project” (NAP3) of the Royal College of Anaesthetists1 contains an overview of the potential benefits of CNB. Although studies are generally underpowered and lack standardisation in design, improved analgesia has been shown repeatedly. Many studies have demonstrated reductions in mortality, with the strongest evidence existing for high-risk patients undergoing major surgery. Other benefitsfor CNB after major surgery include:

  • Reduced infective and non-infective respiratory complications and respiratory failure
  • Reduced cardiovascular complications
  • Reduced gastrointestinal complications (including delayed recovery of normal function)
  • Reduced thromboembolic risk (it is recommended by the National Institute for Health and Clinical Excellence for this reason)2

A shorter length of hospital stay with CNB has only been demonstratedas part of “enhanced recovery” trials, which incorporate a range of other interventions (including planned mobilisation and regularly administered baseline analgesia).

Epidural anaesthesia

Generally, epidural infusions contain an opioid analgesic (usually diamorphine or fentanyl) and a local anaesthetic. Bupivacaine is the most commonly used local anaesthetic. There is some evidence that, in high doses, levobupivacaine could be safer than bupivacaine; however, itis also more expensive. In some centres, this additional cost is justified on the grounds of potential improved patient safety (eg, in the case of accidental administration into the wrong site or overdose). This may be particularly relevant in areas where non-anaesthetists administer epidural blocks.

Because epidural administration requires lower opioid doses than systemic treatment, epidural administration is usually associated with fewer side effects (however, other adverse events — eg, due to the localanaesthetic or the complexity of administration — can occur).

Solutions for epidural administration must be sterile and preservative-free. Standard bags of epidural “mixes” (eg, fentanyl 2µg/ml plus bupivacaine 0.1%) can be purchased from specials manufacturers. Some patients will not tolerate epidural opioids (see adverse effects below) so a local anaesthetic alone can be used (eg, bupivacaine 0.25%).

Although epidurals are administered as continuous infusions in most centres, the use of patient-controlled epidural analgesia (PCEA) is increasing in popularity. PCEA gives the patient a greater degree of control over his or her pain relief and has the potential to minimise adverse effects by limiting doses required, although evidence supportingthis is conflicting.3

Intravenous administration of drugs meant for epidural administrationhas been specified as a “never event” by the Department of Health.4 Adequate training and multidisciplinary working are vital for safe epidural treatment and auditing clinical practice is also important; best practice guidance has recently been updated.5

Sensory and motor block testing

Generally, the aim of epidural anaesthesia is to achieve blockade of sensory nerves, but to avoid motor block.

Sensory block testing is used to assess whether an epidural is working effectively and covering the intended area. Pin prick assessmenthas largely been superseded by cold testing (using either ice or ethyl chloride spray). The area of reduced sensation should cover the wound site and should not routinely exceed T4 (the nipple level); higher blockade can cause hypotension, due to bilateral blockade of upper thoracic (cardiac) sympathetic nerves, or difficulty breathing, caused by blockade of nerve supply to the intercostal muscles. Small adjustments to the block height (or side) can be made gravitationally bychanging a patient’s position, although reducing or discontinuing the infusion may be required until control of block height returns.

Motor block is tested by assessing a patient’s ability to move his orher legs. This is important to determine the extent to which a patient can mobilise and the degree of assistance needed. A sudden onset of motor block can indicate migration of the epidural catheter, epidural abscess or haematoma formation. Some degree of transient motor block is expected when administering opioids in lower thoracic and lumbar epidurals, particularly initially and following bolus doses.

Adverse effects

Respiratory depression and sedation

Respiratory depression and sedation caused by the opioid component ofthe epidural can be minimised by providing supplemental oxygen and encouraging deep breathing exercises. A patient’s level of sedation should be monitored closely since this will give the earliest warning ofpotential respiratory depression.

Trusts should have guidance detailing management of sedation, which is usually measured using the “AVPU score”, an acronym for alert, (responding to) voice, (responding to) pain, and unconscious. If a patient is not alert or responding to voice, particularly if the respiratory rate is also reduced (ie, less than eight breaths per minute), the epidural should be reduced or stopped and naloxone may be required. Naloxone is usually administered as an intravenous bolus followed by continuous infusion due its short half-life.


Commonly, hypotension occurs perioperatively and can be caused by a combination of factors including general anaesthesia, hypovolaemia and epidural infusion of local anaesthetic. Clinicians should assess patients carefully before assuming that hypotension is caused by an epidural. Following exclusion of other potential causes, management options include administration of fluids, reducing or stopping the epidural, or administration of vasopressors (eg, phenylephrine) or inotropes.


Epidural-associated itch can be severe, prolonged and distressing forthe patient. Although this opioid-associated effect is not histamine-related, antihistamines (eg, chlorphenamine) are commonly usedfor its treatment. Ondansetron and low-dose infusions of naloxone have been found to be effective for the treatment of opioid-induced pruritus,so may be considered for the management of epidural-associated itch.3

Nausea and vomiting

Prophylactic and “rescue” antiemetics should be prescribed for patients at high risk of nausea and vomiting in the postoperative period; this includes patients receiving opioids epidurally.6

Risk of permanent injury

Paralysis is a feared complication of epidural analgesia among both healthcare professionals and the general population. Cook and colleaguesreviewed the incidence of major complications of CNB in the UK (eg, epidural abscess or haematoma) and found that the incidence of permanentinjury was between one in 24,000 and one in 54,000 — lower than previously reported in smaller case series.1

Epidural removal

An epidural catheter should only be removed if 12 hours have elapsed since the last dose of low molecular weight heparin (LMWH). A further two hours should be allowed to pass before administering the next dose. Many trusts routinely give prophylactic LMWH at 6pm, allowing a useful window for catheter removal the following day (morning to early afternoon).

Generally, warfarin is stopped before major surgery and will not be restarted until the epidural catheter is removed (for the newer anticoagulants used in orthopaedic surgery, consult local policies or the product literature).

The United Kingdom Clinical Pharmacy Association has produced practical guidance on the removal of epidurals for patients receiving anticoagulants.7


Local anaesthetic toxicity, characterised by convulsions, cardiac arrhythmias and cardiac arrest, is treated with lipid emulsion (Intralipid). Detailed guidance on the management of local anaesthetic toxicity is available on the Association of Anaesthetists of Great Britain and Ireland website.8 Intralipid should be stored in an easily accessible location, made known to nursing staff and prescribers.

Lee Wilson is a consultant pharmacist for pain management and perioperative care and Donald Graham is a consultant anaesthetist for the acute pain team, both at Doncaster and Bassetlaw Hospitals NHS Foundation Trust.


1    Royal College of Anaesthetists. The 3rd National Audit Project of the Royal College of Anaesthetists. Major complications of central neuraxial blocks in the UK. January 2009. (accessed 1 April 2011).

2    National Institute for Health and Clinical Excellence. Venous Thromboembolism — reducing the risk. January 2010. (accessed 1 April 2011).

3    Macintyre P, Scott DA, Schug SA, et al. Acute pain management: scientific evidence (third edition). 2010. (accessed 1 April 2011).

4    Department of Health. The “never events” list 2011/12. February 2011. (accessed 1 April 2011).  

5    Faculty of Pain Medicine of the Royal College of Anaesthetists. Best practice in the management of epidural analgesia in the hospital setting. November 2010. (accessed 1 April 2011).

6    Gan TJ, Meyer TA, Apfel CC, et al. Society for Ambulatory Anesthesia guidelines for the management of postoperative nausea and vomiting. Anesthesia and Analgesia 2007;105:1615–28.

7    UKCPA HAT Group. What are the recommendations for placement/removal of epidural catheters in patients receiving concurrentthromboprophylaxis? April 2010. (accessed 1 April 2011).

8    The Association of Anaesthetists of Great Britain and Ireland. Management of Severe Local Anaesthetic Toxicity. December 2010. (accessed 1 April 2011).


Studying this article will help you gain a better understanding of:

  • The rationale for, and benefits of, central neuraxial blockade
  • The monitoring required for patients undergoing epidural anaesthesia
  • The medicines used for epidural anaesthesia

For discussion

  • Is there a role for a clinical pharmacist within the acute pain team? What multidisciplinary working exists in your hospital?
  • Would you be comfortable advising on the administration of Intralipid for local anaesthetic toxicity (“lipid rescue”)?
  • Are you aware of the protocols for prescribing and administering epidurals in your hospital?

Test Yourself

1    Which of the following is not part of the AVPU scale:
a)    Alert
b)    Responds to voice
c)    Responds to pain
d)    Responds to pressure
e)    Unresponsive

2    Which of the following statements regarding epidural anaesthesia is true:
a)    It should be administered into the cerebrospinal fluid
b)    Motor blockade is a desired effect
c)    Solutions for epidural infusion must contain preservatives
d)    Lipid emulsion can be used to treat local anaesthetic toxicity
e)    The epidural catheter should be removed within 12 hours of the last dose of low molecular weight heparin

3    Which of the following about central neuraxial blockade is not true:
a)    It includes spinal anaesthesia
b)    The height of the block depends on the site of catheter insertion
c)    Diamorphine is never used
d)    It is often used in obstetrics
e)    It can reduce postsurgical cardiovascular complications

4    Which of the following is a characteristic of local anaesthetic toxicity:
a)    Itch
b)    Respiratory depression
c)    Sedation
d)    Nausea
e)    Cardiac arrhythmias

5    Which of the following is not true regarding epidural-associated itch:
a)    It is histamine-related
b)    It is commonly treated with antihistamines
c)    It can be severe
d)    It is usually related to the opioid component of the infusion
e)    It can be treated with ondansetron 


Answers at the bottom of page 2 (PDF).

Citation: Clinical Pharmacist URI: 11083294

Have your say

For commenting, please login or register as a user and agree to our Community Guidelines. You will be re-directed back to this page where you will have the ability to comment.

Recommended from Pharmaceutical Press

RPS publications

Pharmaceutical Press is the publishing division of the Royal Pharmaceutical Society, and is a leading provider of authoritative pharmaceutical information used throughout the world.

  • Print
  • Share
  • Comment
  • Save
  • Print Friendly Version of this pagePrint Get a PDF version of this webpagePDF

Supplementary information

Newsletter Sign-up

Want to keep up with the latest news, comment and CPD articles in pharmacy and science? Subscribe to our free alerts.